---
title: "AIM-V Medium REF AV.200/500 — FDA record Z-1643-2022 | Is It on Recall"
description: "Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated stora"
url: https://isitonrecall.com/recall/fda-device-z-1643-2022-aim-v-medium-ref-av-200-500/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# AIM-V Medium REF AV.200/500 — FDA record Z-1643-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 7, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: AIM-V Medium REF AV.200/500
- **Reason**: Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated storage time.
- **Classification**: Class II
- **Recalling firm**: OXFORD IMMUNOTEC LTD
- **Quantity**: 6 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1643-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1643-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model/Catalog Number: AV.200/500 UDI-DI Code: Not yet assigned Lot Number: 100380 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.: AL, CA, DC, GA, IN, OR, and WA O.U.S.: None

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alabama](https://isitonrecall.com/state/alabama/)
- [California](https://isitonrecall.com/state/california/)
- [District of Columbia](https://isitonrecall.com/state/district-of-columbia/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Sep 7, 2022
- **Recall initiation date**: Jul 7, 2022
- **Center classification date**: Aug 26, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1643-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [OXFORD IMMUNOTEC LTD records](https://isitonrecall.com/brand/oxford-immunotec-ltd/)